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Xanthates as nitrification inhibitors and urea coatingsWalworth, James Lawrence, January 1980 (has links)
Thesis (M.S.)--University of Wisconsin--Madison, 1980. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 74-82).
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Cellulose xanthate : chemistry, manufacture, and possibilities for use in ore flotation /Dewey, Franklin James. January 1934 (has links)
Thesis (M.S.)--Virginia Polytechnic Institute, 1934. / Abstract. Includes bibliographical references (leaves 145-149). Also available via the Internet.
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Illumination and the adsorption of xanthate in the flotation of galena and marmatiteGuarnaschelli, Claudio January 1968 (has links)
The changes in the adsorption characteristics of potassium ethyl xanthate (KEtX) on galena (PbS) and marmatite [(Zn,Fe)S] due to illumination have been investigated.
Studies by others have indicated that: (1) the amount of surfactant adsorbed by a semiconductor depends on its n-type or p-type character, (2) copper activation of sphalerite (ZnS) is required for flotation, (3) sphalerite is a semiconductor with an energy gap of 3.6 eV whereas galena is a semiconductor with an energy gap of 0.3 7 eV.
The amount of xanthate adsorbed from aqueous solution on galena and marmatite was found to depend on both the intensity and photon energy (0.5 to 3.5 eV) of the incident light. In the galena system, increasing the light photon energy above the energy gap value increased adsorption of xanthate. The amount of xanthate adsorbed by the p-type galena was three times the amount adsorbed by the n-type galena. This suggested that the reaction may involve the transfer of an electron from the adsorbate to the adsorbent. The effect of the presence of an oxide film on the surfaces of galenas was also investigated and appeared to be less significant than the type of charge carrier originally dominant in the mineral.
When copper-activated marmatite was illuminated by light with photon energies lower than the intrinsic gap (3.6 eV), adsorption of xanthate was less than when the mineral was kept in darkness. Similar "photodesorption" effects have been reported in the literature. These were explained by excitation of electrons from traps to the conduction band and subsequent recombination with holes in the valence band. Fewer charge carriers would then have been available to participate in the adsorption reactions. Flotation experiments agreed with the adsorption results above. Flotation recovery of activated marmatite dropped ca. 10% when the mineral was illuminated with a high intensity of 0.6 eV photons as compared to the recovery in daylight.
A model that takes into account the surface concentration of electrons and the type and concentration of impurities is discussed. The activity and selectivity of surface reactions are explained in terms of the electrochemical potential, i.e. the Fermi energy level, the actual position and/or displacement of which is affected by the impurities present. / Applied Science, Faculty of / Mining Engineering, Keevil Institute of / Graduate
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The synthesis of macrolactones from [omega]-hydroxyacyl xanthatesAkella, Annapoorna 23 August 1991 (has links)
Graduation date: 1992
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The role of oxygen in xanthate flotation of galena, pyrite, and chalcopyrit.Klymowsky, Irenej Boris January 1968 (has links)
No description available.
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The role of oxygen in xanthate flotation of galena, pyrite, and chalcopyrit.Klymowsky, Irenej Boris January 1968 (has links)
No description available.
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Density functional theory studies of O2, H2O, OH- and xanthates adsorption on platinum antimony (PtSb2) surfacesMangoejane, Samuel Seshupo January 2020 (has links)
Thesis (Ph.D.(Physics)) -- University of Limpopo, 2020 / The effects of O2, H2O and OH− and collectors are the major factors that determine the
flotability behaviour of minerals. In particular, the influence of the chain length variation
on xanthate collectors gives rise to increased recovery rates, and are still the most versatile collector for most minerals. This study explores the bonding behaviour, adsorption energies and electronic properties directly related to the reactivity of O2, H2O and OH−, ethyl xanthates (EX), normal propyl-xanthate (nPX), normal-butyl-xanthate (nBX–) and amyl-xanthate (AX) with the platinum antimony mineral surfaces: (100), (110) and (111) surfaces. We employed the ab-initio quantum mechanical density functional theory to investigate their adsorption and their electronic properties. In order to attain precise calculations, the cut-off energy of 500 eV was used for the bulk PtSb2, which was also transferred to the surfaces. To obtain accurate results the k point used for both the bulk and surfaces were 6x6x6 and 4x4x1, respectively. The bulk relaxation was found to give final lattice parameter of 6.531 Å. The DOS (Density Of States) indicated that both bulk and surfaces of PtSb2 had a metallic character, thereby indicating semiconducting behaviour. In cleaving the surfaces, all possible terminations were considered and the slab thickness was varied to obtain the desired stable surfaces. Their relaxed surface energies were 0.807 J.m-2, 1.077 J.m-2 and 1.074 J.m-2 for the (100), (111) and (110), respectively. These indicated that the (100) surface was the most stable and dominant plane for the platinum antimony. This fact is also observed in other minerals in general that low-index surfaces with lower surface energies indicates structural stability. The DOS showed stability with the EF (Fermi level/ Fermi energy) falling deep into the pseudo gap for all surface. The valence electrons on the surface were 5d96s1 for Pt and 5s25p3 for Sb as depicted from the Mulliken population charges and these electrons were actively involved in the hybridisation. The oxidation showed that the oxygen molecules preferred interacting with the Sb atoms than the Pt atoms for all surfaces. For the (100) surface we found that the Pt-O2peroxide adsorption site gave the strongest adsorption, while for the (110) surface we noted that the Sb2-O-O-Sb3 bridging gave the most exothermic adsorption. The case of the (111) surface showed the Sb2-O-O-Sb2 bridging to give the strongest exothermic adsorption, which dissociated and resulted in atomic bonding. Their atomic charges indicated that the oxygen molecules gain charges from the Pt and Sb atoms. In all cases, PtSb2 Bulk PtSb2 (100), (110) and (111) surfaces
O2, H2O, OH-and Xanthates adsorptions the O2 interacting with Sb gained more charges, thus showing preferential adsorption to the Sb atoms. In addition, the Sb/Pt-bonded oxygens were more negative than the terminal or end-bonded oxygen atom for superoxide modes. These suggested that the 2p-orbital spin-down unoccupied orbital (LUMO) of O2 is fully occupied. The case of H2O molecules adsorptions on the three PtSb2 mineral surfaces indicated that the H2O adsorbed through van der Waals forces, in particular for multi adsorptions by physisorption process for the (100) and the (110) surfaces. However, on the (111) surface we observed chemisorption adsorption. For the (100) surface we found that the H2O-Pt was exothermic, while the H2O-Sb was endothermic and only showed exothermic from 5/8-8/8 H2O/Sb. The case of the (110) surface showed stronger adsorption of H2O on Pt than on Sb atoms, with a weaker adsorption on Sb2 atoms, while the adsorption on the (111) surface was stronger on Sb3 and weaker on Sb2 atoms. The full-coverage for the (110) surface gave –35.00 kJ/mol per H2O molecule, which is similar to the full coverage on the (100) surface (–38.19 kJ/mol per H2O molecule). Furthermore, the full monolayer adsorption on Sb2 and Sb3 for the (111) surface gave much stronger adsorption (–55.54 kJ/mol per H2O). In addition, the full-coverage on the (111) surface (i.e. on Pt1 and all Sb atoms) gave adsorption energy of –54.95 kJ/mol per H2O molecule. The adsorption of hydroxide on the surfaces showed stronger affinity than the water molecules. This suggested that they will bind preferentially over the water molecules. We also found that the OH–preferred the Sb atoms on the (100) surface, with a greater adsorption energy of –576.65 kJ/mol per OH– molecule for full-surface coverage. The (110) surface adsorption energy on full-surface coverage was –541.98 kJ/mol per OH molecule. The (111) surface full-coverage yielded adsorption energy of –579.53 kJ/mol per OH– molecule. The atomic charges related to both hydration and hydroxide adsorption showed charge depletion on both Pt/Sb and O atoms of the H2O and OH–. This suggested that there is a charge transfer into other regions within the orbitals. The adsorption of collectors on the PtSb2 surfaces to investigate their affinity with
surfaces were performed considering different adsorption sites in order to find the most
stable exothermic preferred site. In respect of the (100) surface, we noted that the bridging on Pt and Sb atoms by the collector involved the S atoms for all xanthates. Their
adsorption energies showed that EX had strong affinity with the surface and the order was
as: EX ≈ AX > nBX > nPX. In the case of the (110) surface the bridging on Pt atoms were PtSb2 Bulk PtSb2 (100), (110) and (111) surfaces O2, H2O, OH-
and Xanthates adsorptions the most preferred sites for EX, nPX, nBX and AX. The order of adsorption energies was: nBX > nPX ≈ AX > EX. The (111) surface was observed to have the bridging on Sb2 and Sb3 atoms most exothermic for EX, nBX and AX, while the nPX showed the bridging on Pt1 and Sb3 atoms. The adsorption energies were found to have the nPX more stronger on the surface, with EX weaker and the order decreased as: nPX > nBX > AX > EX. This gave insights in the recovery of the minerals during flotation, that the use of EX or AX may float the platinum antimonide better based on the adsorption trends on the (100) surface, which is the most stable surface plane cleavage for platinum antimonide. The analysis of the electronic structures of the collector on the surface from density of states showed stability bonding of the collector on the surface, due to the EF falling deep into the pseudo gap for collector S atoms and surface Pt and Sb PDOS. The atomic charges computed indicated that the collectors behave as electron donors and acceptors to the Pt and Sb on the surface, respectively for the (100) surface. Interestingly for the (110) surface we observed that both surface Pt and Sb atoms lost charges, with a loss of charges on the collector S atoms. These observations suggested that the collectors S atoms offer their HOMO electrons to Pt and Sb atoms to form bond and simultaneously the Pt and Sb atoms donate their d-orbital and p-orbitals electrons to the LUMO of the collectors to form a back donation covalent bond, respectively. The (111) surface clearly showed that the surface Pt and Sb atoms lose charges to the collector S atoms, suggested a back donation covalent bonds. / National Research Foundation (NRF) and
CSIR (Council for Scientific and Industrial Research) through Centre for High Performance Computing (CHPC)
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Interaction of ethyl xanthate with pyrite and pyrrhotite minerals /Montalti, Marianne. Unknown Date (has links)
Thesis (PhD)--University of South Australia, 1994
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Rate of xanthation of soda-cellulose: an investigation of the rate of xanthation of the soluble cellulose xanthateGriffin, Jerome B. January 1942 (has links)
For the past several years an investigation has been carried out,under the supervision of Dr. P. C. Scherer, of the physical, or chemical reactions which occur in the xanthation of soda-cellulose. A study has been made of the rate of xanthation of the soda-cellulose under various conditions.
Following up the previous work, the present investigation was to determine the rate of xanthation of the soluble cellulose xanthate, using a sodium hydroxide solution as a solvent. By this study it was hoped that further information could be obtained concerning the reaction which occurs when soda-cellulose is treated with carbon disulfide.
It is concluded from the results of this investigation that a definite carbon disulfide-cellulose ratio is reached before cellulose xanthate will assume properties which will render it soluble in a solvent such as a sodium hydroxide solution.
Also, that this carbon disulfide-cellulose ratio will remain constant throughout further xanthation. / M.S.
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Investigation of cellulose xanthateEarnest, George Irving January 1935 (has links)
I have attempted to synthesize cellulose xanthate in anhydrous liquid ammonia, and to analyze the product for combined sodium and sulphur, with the hope of determining the exact chemical composition of each C₆ unit of cellulose xanthate.
It is the purpose of this work to study the xanthation of cellulose with the idea in mind of adding more experimental evidence to the data now available, as to the composition of cellulose xanthate. It is hoped that sufficient evidence will be available at the completion of this problem, to finally enable us to form definite conclusions concerning the actual chemical structure of cellulose xanthate. / M.S.
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